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Thrombophilia MTHFR

Detects MTHFR mutations, used to assess risk for thrombophilia.

3,250 THB

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Thyroid-Stimulating Immunoglobulin

Detects TSI antibodies to diagnose Graves’ disease, an autoimmune thyroid disorder.

26,928 THB

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VCFS/ DiGeorge/CATCH22 by FISH

Detects chromosomal deletions associated with DiGeorge syndrome, a genetic disorder.

8,505 THB

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VISTA Carrier Screening Mini Panel PLUS

Carrier screening for common genetic conditions using next-generation sequencing and additional molecular methods.

35,840 THB

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Whole Exome Sequencing

Detects genetic mutations through whole exome sequencing, used in diagnosing rare genetic disorders.

78,750 THB

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Whole Exome Sequencing Trio analysis

Analyzes the exome of a patient and both parents (trio analysis) to detect genetic disorders.

143,500 THB

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Whole Genome Sequencing Trio analysis

Analyzes the whole genome of a proband and both parents to detect genetic variations and mutations.

217,880 THB

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Wilson Disease Mutation

Identifies mutations associated with Wilson disease, a genetic disorder affecting copper metabolism.

32,400 THB

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